Race modifies default mode connectivity in Alzheimer’s disease

Abstract Background Older African Americans are more likely to develop Alzheimer’s disease (AD) than older Caucasians, and this difference cannot be readily explained by cerebrovascular and socioeconomic factors alone. We previously showed that mild cognitive impairment and AD dementia were associat...

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Main Authors: Maria B. Misiura, J. Christina Howell, Junjie Wu, Deqiang Qiu, Monica W. Parker, Jessica A. Turner, William T. Hu
Format: Article
Language:English
Published: BMC 2020-02-01
Series:Translational Neurodegeneration
Subjects:
Online Access:http://link.springer.com/article/10.1186/s40035-020-0186-4
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author Maria B. Misiura
J. Christina Howell
Junjie Wu
Deqiang Qiu
Monica W. Parker
Jessica A. Turner
William T. Hu
author_facet Maria B. Misiura
J. Christina Howell
Junjie Wu
Deqiang Qiu
Monica W. Parker
Jessica A. Turner
William T. Hu
author_sort Maria B. Misiura
collection DOAJ
description Abstract Background Older African Americans are more likely to develop Alzheimer’s disease (AD) than older Caucasians, and this difference cannot be readily explained by cerebrovascular and socioeconomic factors alone. We previously showed that mild cognitive impairment and AD dementia were associated with attenuated increases in the cerebrospinal fluid (CSF) levels of total and phosphorylated tau in African Americans compared to Caucasians, even though there was no difference in beta-amyloid 1–42 level between the two races. Methods We extended our work by analyzing early functional magnetic resonance imaging (fMRI) biomarkers of the default mode network in older African Americans and Caucasians. We calculated connectivity between nodes of the regions belonging to the various default mode network subsystems and correlated these imaging biomarkers with non-imaging biomarkers implicated in AD (CSF amyloid, total tau, and cognitive performance). Results We found that race modifies the relationship between functional connectivity of default mode network subsystems and cognitive performance, tau, and amyloid levels. Conclusion These findings provide further support that race modifies the AD phenotypes downstream from cerebral amyloid deposition, and identifies key inter-subsystem connections for deep imaging and neuropathologic characterization.
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spelling doaj.art-e6b2e07cd7e348d1b12e59e67e117e442022-12-22T01:31:14ZengBMCTranslational Neurodegeneration2047-91582020-02-019111510.1186/s40035-020-0186-4Race modifies default mode connectivity in Alzheimer’s diseaseMaria B. Misiura0J. Christina Howell1Junjie Wu2Deqiang Qiu3Monica W. Parker4Jessica A. Turner5William T. Hu6Department of Psychology, Georgia State UniversityDepartments of Neurology, Emory UniversityDepartments of Radiology, Emory UniversityDepartments of Radiology, Emory UniversityDepartments of Neurology, Emory UniversityDepartment of Psychology, Georgia State UniversityDepartments of Neurology, Emory UniversityAbstract Background Older African Americans are more likely to develop Alzheimer’s disease (AD) than older Caucasians, and this difference cannot be readily explained by cerebrovascular and socioeconomic factors alone. We previously showed that mild cognitive impairment and AD dementia were associated with attenuated increases in the cerebrospinal fluid (CSF) levels of total and phosphorylated tau in African Americans compared to Caucasians, even though there was no difference in beta-amyloid 1–42 level between the two races. Methods We extended our work by analyzing early functional magnetic resonance imaging (fMRI) biomarkers of the default mode network in older African Americans and Caucasians. We calculated connectivity between nodes of the regions belonging to the various default mode network subsystems and correlated these imaging biomarkers with non-imaging biomarkers implicated in AD (CSF amyloid, total tau, and cognitive performance). Results We found that race modifies the relationship between functional connectivity of default mode network subsystems and cognitive performance, tau, and amyloid levels. Conclusion These findings provide further support that race modifies the AD phenotypes downstream from cerebral amyloid deposition, and identifies key inter-subsystem connections for deep imaging and neuropathologic characterization.http://link.springer.com/article/10.1186/s40035-020-0186-4Alzheimer’s diseaseCognitive impairmentFunctional connectivityDefault mode networkDisparities
spellingShingle Maria B. Misiura
J. Christina Howell
Junjie Wu
Deqiang Qiu
Monica W. Parker
Jessica A. Turner
William T. Hu
Race modifies default mode connectivity in Alzheimer’s disease
Translational Neurodegeneration
Alzheimer’s disease
Cognitive impairment
Functional connectivity
Default mode network
Disparities
title Race modifies default mode connectivity in Alzheimer’s disease
title_full Race modifies default mode connectivity in Alzheimer’s disease
title_fullStr Race modifies default mode connectivity in Alzheimer’s disease
title_full_unstemmed Race modifies default mode connectivity in Alzheimer’s disease
title_short Race modifies default mode connectivity in Alzheimer’s disease
title_sort race modifies default mode connectivity in alzheimer s disease
topic Alzheimer’s disease
Cognitive impairment
Functional connectivity
Default mode network
Disparities
url http://link.springer.com/article/10.1186/s40035-020-0186-4
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